纳米线
碳纳米管
材料科学
纳米技术
氢
原子单位
碳纤维
化学工程
化学
复合数
物理
复合材料
量子力学
工程类
有机化学
作者
Zichu Zhang,Rui-Hong Xie,Xuefeng Liang,Feng Zhang,Hao Yang,Meng-Ke Zou,Lili Zhang,Chao Shi,Hui–Ming Cheng,Leining Zhang,Chang Liu,Leining Zhang,Chang Liu
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-05-14
卷期号:25 (21): 8612-8618
被引量:2
标识
DOI:10.1021/acs.nanolett.5c01381
摘要
Phase-pure ultrafine W2C nanostructures are promising electrocatalysts but face synthesis challenges due to unclear formation mechanisms and harsh thermodynamics. Here, we reveal the formation mechanism of ultrathin W2C nanowires (NWs) confined in the cavity of single-wall carbon nanotubes (SWCNTs) at the atomic scale by combined in situ transmission electron microscopy and density functional theory calculations. It was found that the hollow core of SWCNTs can control the phase, axial orientation, and diameter of W2C NWs. Leveraging this mechanism, we synthesized SWCNT-encapsulated W2C NWs, WS2-W2C heterostructures, and WS2 NWs (1D@1D), which assembled into free-standing hybrid films. The integrated W2C NWs@SWCNT membrane was primarily tested, exhibiting a low overpotential of 44 mV to reach a current density of 10 mA cm-2 and outstanding durability (500 h at a high current density of 250 mA cm-2 in acidic conditions).
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